enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12.The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond.

  3. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

    The molecular formula C 6 H 12 may refer to following structural isomers: ... 1-Hexene; 2-Hexene; 3-Hexene; Methylpentenes. 2-Methyl-1-pentene; 3-Methyl-1-pentene; 4 ...

  4. 3-Hexyne - Wikipedia

    en.wikipedia.org/wiki/3-Hexyne

    3-Hexyne is the organic compound with the formula C 2 H 5 CCC 2 H 5. This colorless liquid is one of three isomeric hexynes. 3-Hexyne forms with 5-decyne, 4-octyne, and 2-butyne a series of symmetric alkynes. It is a reagent in organometallic chemistry. [1] Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [2]

  5. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    It consists of several isomeric compounds having the formula C 6 H 10. The linear and branched members are: 1-Hexyne (n-butylacetylene) 2-Hexyne (methylpropylacetylene)

  6. 1-Hexene - Wikipedia

    en.wikipedia.org/wiki/1-Hexene

    1-Hexene (hex-1-ene) is an organic compound with the formula C 6 H 12.It is an alkene that is classified in industry as higher olefin and an alpha-olefin, the latter term meaning that the double bond is located at the alpha (primary) position, endowing the compound with higher reactivity and thus useful chemical properties. 1-Hexene is an industrially significant linear alpha olefin.

  7. 1-Hexyne - Wikipedia

    en.wikipedia.org/wiki/1-Hexyne

    The hexyl derivative is common test substrate because it is conveniently volatile. It undergoes deprotonation at C-3 and C-1 with butyl lithium: HC 2 C 4 H 9 + 2 BuLi → LiC 2 CH(Li)C 3 H 7 + 2 BuH. This reaction allows alkylation at the 3-position. [2] Catechol borane adds to 1-hexyne to give the 1-hexenyl borane. [3]

  8. Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexene

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  9. 2-Hexyne - Wikipedia

    en.wikipedia.org/wiki/2-Hexyne

    2-Hexyne can be semihydrogenated to yield 2-hexene or fully hydrogenated to hexane. [3] With appropriate noble metal catalysts it can selectively form cis-2-hexene. [4] 2-Hexyne can act as a ligand on gold atoms. [5] With strong sulfuric acid, the ketone 2-hexanone is produced. However this reaction also causes polymerization and charring. [6]